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HRID 1615592作成日:2026年10月25日

Water → 2-Chloro-7-iodo-5-methyl-5H-pyrrolo[3,2-d]pyrimidine

https://huagongshe.com/reaction/1615592

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Methyl iodideHCID 6328—
反応物Sodium HydroxideHCID 14798—
反応物2-chloro-7-iodo-5H-pyrrolo[3,2-d]pyrimidineHCID 45588465—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒DichloromethaneHCID 6344—
生成物2-Chloro-7-iodo-5-methyl-5H-pyrrolo[3,2-d]pyrimidineHCID 7130774070%

反応手順

To a suspension of 2-chloro-7-iodo-5H-pyrrolo[3,2-d]pyrimidine (1 g, 3.57 mmol, 1.0 eq.) and NaOH (0.430 mg, 10.73 mmol, 3.0 eq.) in DCM (28 ml) was added iodomethane (0.66 g, 4.6 mmol, 1.3 eq.) and tetrabutylammonium bromide (0.116 g, 0.36 mmol, 0.1 eq.). The reaction mixture was stirred at room temperature overnight. Water was poured in and the aqueous layer extracted with ethyl acetate (2 times). The combined organic layers were then dried over Na2SO4. After filtration and evaporation the yellow residue was triturated with a mixture of ethyl acetate/petroleum spirit (1:2) to give the product as a white solid (0.73 g, 70%). 1H NMR (DMSO, 300 MHz): 8.99 (s, 1H), 8.17 (s, 1H), 3.94 (s, 3H); LRMS (EI): m/z calcd for [M+H]+ 293.93 found 294.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08765755B2
出典データセットuspto-grants-2014_07
ORD IDord-fe3886800d234df6b71bc76b5b67110f
出典メモuspto-grants-2014_07